• The PAH enzyme functions in liver as homo-tetramers to hydroxylate phenylalanine (Phe) into tyrosine and requires the co-factor tetrahydrobiopterin for catalysis. Phenylalanine hydroxylase (PAH) deficiency prevents the conversion of Phe to tyrosine. PAH deficiency results in hyperphenylalaninemia (HPA) and irreversible neurological consequences if left untreated.
• The exon 12 of mouse Pah gene was replaced by human PAH exon 12 with the R408W mutation in B-hPAH*R408W mice.
• Mouse Pah mRNA was only detectable in wild-type mice, human PAH mRNA was exclusively detectable in homozygous B-hPAH*R408W mice. Human PAH exon 12 replacement does not affect the normal splicing of mRNA.
• PAH protein expression was detected in the liver and kidney from both wild-type mice and homozygous B-hPAH*R408W mice, as the antibody used showed cross-reactivity between human and mouse PAH. Moreover, PAH protein expression of wild-type mice was higher than that of homozygous B-hPAH*R408W mice.
• Application: This product is used for pharmacodynamics evaluation of Phenylketonuria (PKU).

Gene targeting strategy for B-hPAH*R408W mice. The exon 12 of mouse Pah gene was replaced by human PAH exon 12 with the R408W mutation in B-hPAH*R408W mice.

Strain specific analysis of PAH mRNA expression in wild-type C57BL/6JNifdc mice and B-hPAH*R408W mice by RT-PCR. Liver RNA were isolated from wild-type C57BL/6JNifdc mice (+/+) and homozygous B-hPAH*R408W mice (H/H), then cDNA libraries were synthesized by reverse transcription, followed by PCR with mouse or human PAH primers. Mouse Pah mRNA was only detectable in wild-type mice. Human PAH mRNA was exclusively detectable in homozygous B-hPAH*R408W mice. The point mutation in homozygous B-hPAH*R408W mice was confirmed via Sanger Sequencing.

Western blot analysis of PAH protein expression in homozygous B-hPAH*R408W mice. Various tissue lysates were collected from wild-type C57BL/6JNifdc mice (+/+) and homozygous B-hPAH*R408W mice (H/H), and then analyzed by western blot with anti-PAH antibody (abcam, ab178430). 40 μg total proteins were loaded for western blot analysis. PAH protein expression was detected in the liver and kidney from both wild-type mice and homozygous B-hPAH*R408W mice (indicated by the red arrow), as the antibody used showed show cross-reactivity between human and mouse PAH. Moreover, PAH protein expression in both liver and kidney from wild-type mice were higher than those from homozygous mice.